Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Service de Génétique Moléculaire, |
RCV001270382 | SCV001450662 | likely pathogenic | Autism spectrum disorder due to AUTS2 deficiency | 2020-05-27 | no assertion criteria provided | clinical testing |